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司帕吉林:一种新型抗肿瘤抗生素。

Spergualin: a new antitumour antibiotic.

作者信息

Umezawa K, Takeuchi T

机构信息

Institute of Microbial Chemistry, Tokyo.

出版信息

Biomed Pharmacother. 1987;41(5):227-32.

PMID:3499181
Abstract

Spergualin was isolated from the culture filtrate of Bacillus laterosporus as an antitumour substance. It had a unique structure and was shown to have chemotherapeutic effects on mouse transplantable leukaemias such as L-1210, P-388, P-815, C-1489, EL-4 and RL male 1. It was especially effective to L-1210 leukaemia and the leukaemia-bearing mice were even curable by the optimal dose of this drug. When the spergualin-treated cured mice were inoculated again by L-1210 cells, those leukaemic cells did not grow in the animals suggesting that specific immunity to L-1210 had been induced. In this induction of immunity cytotoxic T lymphocytes were suggested to be involved. Cytostatic effect of spergualin in cell culture was dependent on the content of amine oxidase in serum. In the study of structure-activity relationship, the 15-hydroxy group was found to be not necessary, while the spermidine moiety was essential for antitumour activity. 15-Deoxy derivative of spergualin was found to be more potent in antitumour activity.

摘要

角鲨胍是从侧孢芽孢杆菌的培养滤液中分离出来的一种抗肿瘤物质。它具有独特的结构,对小鼠可移植性白血病如L-1210、P-388、P-815、C-1489、EL-4和RL雄性1等显示出化疗作用。它对L-1210白血病特别有效,携带白血病的小鼠用该药物的最佳剂量甚至可以治愈。当用角鲨胍治疗治愈的小鼠再次接种L-1210细胞时,那些白血病细胞在动物体内不生长,这表明对L-1210产生了特异性免疫。在这种免疫诱导中,细胞毒性T淋巴细胞被认为参与其中。角鲨胍在细胞培养中的细胞抑制作用取决于血清中胺氧化酶的含量。在构效关系研究中,发现15-羟基不是必需的,而亚精胺部分对抗肿瘤活性至关重要。角鲨胍的15-脱氧衍生物在抗肿瘤活性方面更有效。

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